The rate of sister chromatid exchanges parallel to spontaneous chromosome breakage in Fanconi's anemia and to trenimon-induced aberrations in human lymphocytes and fibroblasts
- 1 January 1975
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 29 (3) , 201-206
- https://doi.org/10.1007/bf00297624
Abstract
The incidence of structural chromosome aberrations and the rate of sister chromatid exchanges (SCE) was investigated in lymphocyte cultures from a patient with typical Fanconi's anemia and his parents. The rate of SCEs was found to be normal. In experiments with the alkylating agent Trenimon the SCE rates proved to be a sensitive indicator for the induction of structural aberrations: in presence of an induced aberration rate half as high as the spontaneous rate in the Fanconi's anemia case, the rate of SCEs was found to be quintupled. Dose-effect relationships for the induction of SCE rates by Trenimon were studied over a wide dose range in lymphocyte and fibroblast cultures. The results reflect the same difference in sensitivity earlier observed in the induction of structural chromosome aberrations, fibroblasts being far more sensitive.Keywords
This publication has 10 references indexed in Scilit:
- Frequency and distribution of sister-chromatid exchanges in a case of Fanconi's anemiaHuman Genetics, 1975
- A Manyfold Increase in Sister Chromatid Exchanges in Bloom's Syndrome LymphocytesProceedings of the National Academy of Sciences, 1974
- New Giemsa method for the differential staining of sister chromatidsNature, 1974
- Sister Chromatid Exchanges, Indices of Human Chromosome Damage and Repair: Detection by Fluorescence and Induction by Mitomycin CProceedings of the National Academy of Sciences, 1974
- Chromatidaustausch und Heterochromatinveränderungen menschlicher Chromosomen nach BUdR-MarkierungHuman Genetics, 1974
- Microfluorometric Detection of Deoxyribonucleic Acid Replication in Human Metaphase ChromosomesProceedings of the National Academy of Sciences, 1973
- Chemical mutagenesis the Chinese hamster bone marrow as an in vivo test systemHuman Genetics, 1971
- [Chromosal fragility in familial panmyelopathy (Fanconi type)].1965
- Chromosomal Breakage in a Rare and Probably Genetically Determined Syndrome of ManScience, 1965
- Spontane Chromosomenaberrationen bei familiärer PanmyelopathieHuman Genetics, 1964